Compliance Clinical Trials Assistant at IQVIA

الوصف الوظيفي:

أحدث معلومات الوظائف من IQVIA لمنصب Compliance Clinical Trials Assistant. If the Compliance Clinical Trials Assistant الشاغرة في قطر تتوافق مع مؤهلاتك، يرجى تقديم أحدث طلب أو سيرة ذاتية مباشرة من خلال بوابة وظائف Jobkos المحدثة.

يرجى ملاحظة أن التقديم على وظيفة قد لا يكون سهلاً دائماً، حيث يجب على المرشحين الجدد استيفاء مؤهلات ومتطلبات معينة تحددها الشركة. نأمل أن تكون الفرصة المهنية في IQVIA لمنصب Compliance Clinical Trials Assistant أدناه تتوافق مع مؤهلاتك.

We are seeking an **experienced Compliance Clinical Trials Assistant** to join our **cFSP (sponsor-dedicated) team in EMEA.** Candidates are required to have **previous compliance experience within clinical trials** to be considered. **Key Responsibilities** + Document oversight - managing and organising essential trial documents (e.g., Trial Master File / TMF) + Regulatory compliance support - ensuring studies follow guidelines like GCP (Good Clinical Practice), SOPs, and regulatory requirements + Audit and inspection readiness - supporting preparation for audits or inspections from regulators (e.g., MHRA, FDA) + Tracking and reporting - monitoring compliance metrics, deviations, and quality issues + Process improvement - identifying gaps and helping improve compliance processes **What We're Looking For** + Previous compliance experience within clinical trials required. + Candidate must speak English + Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH). + Degree in life sciences or equivalent industry experience. **Please note:** This role is not eligible for visa sponsorship and candidates must hold valid right to work for الدولة of residence. Apply today and forge a career with greater purpose, make an impact, and never stop learning! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled

معلومات الوظيفة:

• الشركة: IQVIA
• المنصب: Compliance Clinical Trials Assistant
• مكان العمل: قطر
• الدولة: QA

كيفية تقديم الطلب:

بعد قراءة وفهم المعايير ومتطلبات الحد الأدنى من المؤهلات الموضحة في معلومات الوظيفة Compliance Clinical Trials Assistant at the office قطر أعلاه، أكمل فوراً ملفات طلب الوظيفة مثل خطاب التقديم، السيرة الذاتية، نسخة من الشهادة الجامعية، كشف الدرجات، والملاحق الأخرى كما هو موضح أعلاه. أرسلها عبر رابط الصفحة التالية أدناه.

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